Reaktionsgleichung
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([N:6]=[CH:7][C:8]([NH:12][NH2:13])=[N:9]2)=[CH:4][CH:3]=1.[CH3:14][C:15](O)=O>O>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([N:6]=[CH:7][C:8]3[N:9]2[C:14]([CH3:15])=[N:13][N:12]=3)=[CH:4][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 7-bromo-2-hydrazinylquinoxaline (200 mg, 0.84 mmol) and AcOH (5 mL) was refluxed overnight. After cooling to r.t., the mixture was treated with water (10 mL); the solid was collected on a filter and dried by vacuum to give 8-bromo-1-methyl-[1,2,4]triazolo[4,3-a]quinoxaline as gray solid (200 mg, yield: 91.0%).
Aufarbeitung
- temperaturewas refluxed overnight
- customthe solid was collected on
- filtrationa filter
- customdried by vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-992eb34c765e4fa783bacf5e677d8d00
- Quelldatensatz
- uspto-grants-2015_11
- Patentnummer
- US09181264B2
Verknüpfte Notizen
Wird geladen…